Canonical Allele Identifier: CA645552577
Gene: CDKN2A HGNC NCBI

Linked Data

COSMIC: COSM13971

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21971203delinsTA , CM000671.2:g.21971203delinsTA GRCh38
NC_000009.11:g.21971202delinsTA , CM000671.1:g.21971202delinsTA GRCh37
NC_000009.10:g.21961202delinsTA NCBI36
NG_007485.1:g.28289delinsTA , LRG_11:g.28289delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000304494.10:c.156delinsTA MANE Select ENSP00000307101.5:p.Met52IlefsTer?
ENST00000404796.3:c.348-58230delinsTA ENSP00000385916.2:n.348-58230delinsTA
ENST00000579755.2:c.199delinsTA MANE Plus Clinical ENSP00000462950.1:p.Asp67Ter
ENST00000304494.9:c.156delinsTA ENSP00000307101.5:p.Met52IlefsTer?
ENST00000361570.4:c.199delinsTA ENSP00000355153.4:p.Asp67Ter
ENST00000380150.2:n.130delinsTA
ENST00000380151.3:c.430delinsTA ENSP00000369496.3:n.430delinsTA
ENST00000404796.2:c.348-58230delinsTA ENSP00000385916.2:n.348-58230delinsTA
ENST00000479692.2:c.3delinsTA ENSP00000466887.1:p.Met1IlefsTer?
ENST00000494262.5:c.3delinsTA ENSP00000464952.1:p.Met1IlefsTer?
ENST00000497750.1:c.3delinsTA ENSP00000468510.1:p.Met1IlefsTer?
ENST00000498124.1:c.156delinsTA ENSP00000418915.1:p.Met52IlefsTer?
ENST00000498628.6:c.3delinsTA ENSP00000467857.1:p.Met1IlefsTer?
ENST00000530628.2:c.199delinsTA ENSP00000432664.2:p.Asp67Ter
ENST00000578845.2:c.3delinsTA ENSP00000467390.1:p.Met1IlefsTer?
ENST00000579122.1:c.156delinsTA ENSP00000464202.1:p.Met52IlefsTer?
ENST00000579755.1:c.199delinsTA ENSP00000462950.1:p.Asp67Ter
NM_000077.4:c.156delinsTA , LRG_11t1:c.156delinsTA NP_000068.1:p.Met52IlefsTer?
NM_001195132.1:c.156delinsTA NP_001182061.1:p.Met52IlefsTer?
NM_058195.3:c.199delinsTA , LRG_11t2:c.199delinsTA NP_478102.2:p.Asp67Ter
NM_058197.4:c.430delinsTA NP_478104.2:n.430delinsTA
XM_005251343.1:c.3delinsTA XP_005251400.1:p.Met1IlefsTer?
XM_011517675.1:c.156delinsTA XP_011515977.1:p.Met52IlefsTer?
XM_011517676.1:c.156delinsTA XP_011515978.1:p.Met52IlefsTer?
XM_011517679.1:c.3delinsTA XP_011515981.1:p.Met1IlefsTer?
XR_929159.1:n.557delinsTA
XR_929161.1:n.346delinsTA
XR_929162.1:n.346delinsTA
XR_929163.1:n.295delinsTA
XR_929164.1:n.78delinsTA
NM_001363763.1:c.3delinsTA NP_001350692.1:p.Met1IlefsTer?
XM_011517675.2:c.156delinsTA XP_011515977.1:p.Met52IlefsTer?
XM_011517676.2:c.156delinsTA XP_011515978.1:p.Met52IlefsTer?
XR_929159.2:n.486delinsTA
NM_001363763.2:c.3delinsTA NP_001350692.1:p.Met1IlefsTer?
NM_000077.5:c.156delinsTA MANE Select NP_000068.1:p.Met52IlefsTer?
NM_001195132.2:c.156delinsTA NP_001182061.1:p.Met52IlefsTer?
NM_058195.4:c.199delinsTA MANE Plus Clinical NP_478102.2:p.Asp67Ter
NM_058197.5:c.*79delinsTA NP_478104.2:n.*79delinsTA